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1 ramming procedures that yield low numbers of induced pluripotent stem cells.
2 epigenome in single embryonic stem cells and induced pluripotent stem cells.
3 embryonic fibroblasts are reprogrammed into induced pluripotent stem cells.
4 from individuals with nonsyndromic ASD using induced pluripotent stem cells.
5 s in cerebral organoids generated from human-induced pluripotent stem cells.
6 878 and small populations of fibroblasts and induced pluripotent stem cells.
7 conversion of mouse embryonic stem cells and induced pluripotent stem cells.
8 topoietic abnormalities with patient-derived induced pluripotent stem cells.
9 from human neural progenitor cells and human induced pluripotent stem cells.
10 ecting ducts, stroma, and vasculature - from induced pluripotent stem cells.
11 t, from mouse embryonic stem cells and human induced pluripotent stem cells.
12 or by reprogramming somatic cells to become induced pluripotent stem cells.
13 in protocols for neuron differentiation from induced pluripotent stem cells allowed us to elucidate t
14 , A243T) were generated from patient-derived induced pluripotent stem cells and compared with wild-ty
15 diomyocytes derived from nontransgenic human induced pluripotent stem cells and generated tissues of
17 bo-H in stem cells (embryonic stem cells and induced pluripotent stem cells) and various normal and c
18 multiple hPSC lines, including embryonic and induced pluripotent stem cells, and it takes approximate
21 he redifferentiation of four patient-derived induced pluripotent stem cells as a model for the onset
23 ed a frontotemporal dementia patient-derived induced pluripotent stem cell carrying the Tau P301L mut
24 nd facilitates the generation of more robust induced pluripotent stem cells, characterized by enhance
28 el in HEK293 cells and also overexpressed in induced pluripotent stem cells derived cardiomyocytes (i
29 ticipants: Neurons differentiated from human-induced pluripotent stem cells derived from 4 individual
30 glial progenitor cells (GPCs) produced from induced pluripotent stem cells derived from patients wit
31 t and structural interconnectivity, based on induced pluripotent stem cells derived from the respecti
32 ncoded by PCSK1) were reduced in PWS patient induced pluripotent stem cell-derived (iPSC-derived) neu
33 21085 on expression of nearby genes in human induced pluripotent stem cell-derived (iPSC-derived) neu
34 d pluripotent stem cells to generate a human-induced pluripotent stem cell-derived cardiac muscle pat
35 al, and force generation properties of human-induced pluripotent stem cell-derived cardiac tissues.
36 r synchronization within maturing, unlabeled induced pluripotent stem cell-derived cardiomyocyte cult
42 nclinical studies of drug effects with human induced pluripotent stem cell-derived cardiomyocytes (hi
44 g rate and decreased beat amplitude in human induced pluripotent stem cell-derived cardiomyocytes (hi
45 eate biological pacemakers in animal models, induced pluripotent stem cell-derived cardiomyocytes (iP
46 onditions to generate EHM from embryonic and induced pluripotent stem cell-derived cardiomyocytes and
47 support the seeding and engraftment of human induced pluripotent stem cell-derived cardiomyocytes and
48 tion of functionalvs remodeling signaling in induced pluripotent stem cell-derived cardiomyocytes and
49 monstrated that commercially available human induced pluripotent stem cell-derived cardiomyocytes are
50 and also supports the use of isogenic human induced pluripotent stem cell-derived cardiomyocytes as
52 d characterized the functional properties of induced pluripotent stem cell-derived cardiomyocytes fro
53 d characterized the functional properties of induced pluripotent stem cell-derived cardiomyocytes fro
54 regulated in rodent cardiomyocytes and human induced pluripotent stem cell-derived cardiomyocytes in
56 modeling and heart repair from embryonic and induced pluripotent stem cell-derived cardiomyocytes und
57 2 expression produced a functional rescue in induced pluripotent stem cell-derived cardiomyocytes wit
58 d was seeded with approximately 50 000 human-induced pluripotent stem cell-derived cardiomyocytes, sm
60 ed the role of TLR3-IFN immunity using human induced pluripotent stem cell-derived cardiomyocytes.
61 s, adult rat ventricular myocytes, and human induced pluripotent stem cell-derived CMs, decreasing ex
62 ouse cells, patient-derived fibroblasts, and induced pluripotent stem cell-derived dopaminergic neuro
64 isease in the lung, our study indicates that induced pluripotent stem cell-derived endothelial cells
66 larizing native intestinal matrix with human induced pluripotent stem cell-derived epithelium and hum
67 mammalian cells, including in vitro cultured induced pluripotent stem cell-derived forebrain neurons
68 se three molecules were downregulated in the induced pluripotent stem cell-derived forebrain neurons
69 tylhydroxytoluene, in endocrine-active human-induced pluripotent stem cell-derived foregut epithelial
70 DE11A), and lithium decreases PDE11A mRNA in induced pluripotent stem cell-derived hippocampal neuron
71 e examined the BM homing properties of human induced pluripotent stem cell-derived HSPCs (hiPS-HSPCs)
72 ellularized rat intestinal matrix with human induced pluripotent stem cell-derived intestinal epithel
73 s and specific ones are deregulated in human-induced pluripotent stem cell-derived MNs carrying the F
74 phenotype in patient-derived fibroblasts and induced pluripotent stem cell-derived motor neurons.
77 neuronal stretch injury model employs human induced pluripotent stem cell-derived neurons (hiPSCNs)
78 in schizophrenia-associated vs control human-induced pluripotent stem cell-derived neurons and 1199 g
79 e morphology of mice hippocampal neurons and induced pluripotent stem cell-derived neurons from a pat
81 xplored the underlying pathophysiology using induced pluripotent stem cell-derived neurons from AS pa
82 ble knockdown of Parkin or SLP-2, as well as induced pluripotent stem cell-derived neurons from Parki
83 d mitophagy, which is also apparent in human induced pluripotent stem cell-derived neurons, a disease
84 t possess greater protective effect in human induced pluripotent stem cell-derived neurons, protectin
86 fashion, but also exacerbated cell death in induced pluripotent stem cell-derived primary human neur
87 e have established conditions by which human induced pluripotent stem cell-derived sensory neurons ca
88 channel expressed in either rodent or human induced pluripotent stem cell-derived sensory neurons in
89 ssion of type III neuregulin-1 (TIIINRG1) in induced pluripotent stem cell-derived sensory neurons st
91 al ordering of human embryonic stem cell and induced pluripotent stem cell-derived single-cell gene e
92 ed doxorubicin-induced cytotoxicity in human induced pluripotent stem cells-derived cardiomyocytes (i
95 an cardiac phenotypes from data generated in induced-pluripotent-stem-cell-derived myocytes from fami
96 ression of Nudt21 enhanced the generation of induced pluripotent stem cells, facilitated transdiffere
97 cells and shares conserved domains with the induced pluripotent stem cell factor Lin28 in mammals.
100 found that human neurons differentiated from induced pluripotent stem cells from patients with Rett s
101 rved in neural progenitor cells derived from induced pluripotent stem cells from schizophrenia patien
102 standards of access to and quality of human induced pluripotent stem cells has lagged behind their u
106 ntional hESC and transgene-independent human induced pluripotent stem cell (hiPSC) lines could be rev
107 in a discovery cohort of 25 phenotyped human induced pluripotent stem cell (hiPSC) lines revealed uni
109 aimed to establish a patient-specific human induced pluripotent stem cell (hiPSC) model of CPVT2 and
112 e compounds, gentamicin and PTC124, in human-induced pluripotent stem cell (hiPSC)-derived cardiomyoc
113 bB2/4 mouse model of SZ, as well as in human induced pluripotent stem cell (hiPSC)-derived forebrain
118 ulation of cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs), 41 were accu
119 o address this, we generated panels of human induced pluripotent stem cells (hiPSCs) and hiPSC-derive
120 w using a stage-matching approach that human induced pluripotent stem cells (hiPSCs) and human embryo
121 bility to generate cardiomyocytes from human induced pluripotent stem cells (hiPSCs) and human embryo
124 loading/dye transfer assay showed that human induced pluripotent stem cells (hiPSCs) contained functi
125 e cells can be generated in vitro from human induced pluripotent stem cells (hiPSCs) derived from pat
126 ed cardiac tissue (LF-ECT) composed of human induced pluripotent stem cells (hiPSCs) derived multiple
127 activity that can specifically detect human induced pluripotent stem cells (hiPSCs) down to a spiked
131 otocols for hepatic differentiation of human induced pluripotent stem cells (hiPSCs) result in low yi
139 vo, and is sufficient to differentiate human induced pluripotent stem cells into electrophysiological
141 , we transplanted TM-like cells derived from induced pluripotent stem cells into the anterior chamber
144 f7 at cilia tips detected in fibroblasts and induced pluripotent stem cell (iPSC) 3D optic cups deriv
145 employed isogenic human RTT patient-derived induced pluripotent stem cell (iPSC) and MeCP2 short hai
147 2/3 significantly improves the efficiency of induced pluripotent stem cell (iPSC) generation by the Y
148 of wild-type and mutant RTT patient-specific induced pluripotent stem cell (iPSC) line carrying the V
149 In this study, we derived a collection of induced pluripotent stem cell (iPSC) lines capturing a r
151 g and gene expression profiling of 215 human induced pluripotent stem cell (iPSC) lines from differen
153 ncy may lead to deleterious DNA mutations in induced pluripotent stem cell (iPSC) lines, which would
156 s of the study were to establish an in vitro induced pluripotent stem cell (iPSC) model of TTS, to te
158 ation of personalized medicine through human induced pluripotent stem cell (iPSC) technology can be a
161 atient brain specimens, we took advantage of induced pluripotent stem cell (iPSC) technology to model
162 iR-146a was significantly upregulated in SMA induced pluripotent stem cell (iPSC)-derived astrocytes
164 and shorten the action potential duration in induced pluripotent stem cell (iPSC)-derived cardiomyocy
165 estigated the therapeutic potential of human induced pluripotent stem cell (iPSC)-derived cells at tw
167 inst PD-related genetic mutations in patient induced pluripotent stem cell (iPSC)-derived DAergic neu
168 ntate gyrus (DG) neurons differentiated from induced pluripotent stem cell (iPSC)-derived fibroblasts
169 f cardiofaciocutaneous syndrome (CFC), in an induced pluripotent stem cell (iPSC)-derived model of hu
170 etecting analytes secreted from single human induced pluripotent stem cell (iPSC)-derived neural cell
172 tissue engineered blood vessel (TEBV) using induced pluripotent stem cell (iPSC)-derived SMCs from a
174 to generate oligodendrocytes (OL) from human induced pluripotent stem cells (iPSC) are currently lack
176 ion, we compared mitochondrial metabolism in induced pluripotent stem cells (iPSC) from 5 healthy ind
179 Here we report the differentiation of human induced pluripotent stem cells (iPSC) into microglia-lik
180 lerosis complex (TSC) and LAM (TSC-LAM) into induced pluripotent stem cells (iPSC), followed by selec
181 blasts and motor neurons differentiated from induced pluripotent stem cells (iPSC-MNs) demonstrate ab
184 igated the innate immune properties of human induced-pluripotent stem cell (iPSC)-derived RPE cells,
186 embryoid body (EB) cells] from primed-state induced pluripotent stem cells (iPSCs) after a 72-hour t
187 yotrophic lateral sclerosis (ALS) with human induced pluripotent stem cells (iPSCs) aims to reenact e
188 wo complementary approaches, patient-derived induced pluripotent stem cells (iPSCs) and conditional E
189 s in two complex processes: reprogramming to induced pluripotent stem cells (iPSCs) and hematopoiesis
190 s (n = 91) and used their tissue to generate induced pluripotent stem cells (iPSCs) and hepatocyte-li
193 mergence of novel technologies such as human induced pluripotent stem cells (iPSCs) and nuclease-medi
194 bility to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the subsequen
198 used frontotemporal dementia patient-derived induced pluripotent stem cells (iPSCs) carrying the Tau
199 al progenitors that were differentiated from induced pluripotent stem cells (iPSCs) derived from indi
201 ysis of murine and human retinoblastomas and induced pluripotent stem cells (iPSCs) derived from muri
207 is required for the efficient generation of induced pluripotent stem cells (iPSCs) from murine embry
210 urodevelopment, the present study used human induced pluripotent stem cells (iPSCs) from RTT and cont
212 ere we use in vitro differentiation of human induced pluripotent stem cells (iPSCs) generated from pa
216 ial reparative abilities of EVs derived from induced pluripotent stem cells (iPSCs) have not been dir
219 of human leukocyte antigen (HLA)-homozygous-induced pluripotent stem cells (iPSCs) is considered a f
220 e reprogramming of differentiated cells into induced pluripotent stem cells (iPSCs) is usually achiev
221 enerate and characterise cardiomyocytes from induced pluripotent stem cells (iPSCs) of RA patients.
222 ing, xenotransplantation and genome editing, Induced pluripotent stem cells (iPSCs) present a range o
224 ase (SCD) genetic defect in patient-specific induced Pluripotent Stem Cells (iPSCs) provides a potent
225 functional CS neural networks from human CS induced pluripotent stem cells (iPSCs) providing a new t
227 , we show that astrocytes derived from human induced pluripotent stem cells (iPSCs) support the repli
228 generated from schizophrenic patient-derived induced pluripotent stem cells (iPSCs) that have been de
229 form based on a genetically diverse panel of induced pluripotent stem cells (iPSCs) that reproduces s
230 entified variants through differentiation of induced pluripotent stem cells (iPSCs) to study cellular
232 ebral organoids derived from control and MDS-induced pluripotent stem cells (iPSCs) using time-lapse
235 organoids derived from schizophrenia patient induced pluripotent stem cells (iPSCs) with a DISC1 muta
236 rivation of functional airway organoids from induced pluripotent stem cells (iPSCs) would provide val
238 sing VCP knockdown neuroblastoma cell lines, induced pluripotent stem cells (iPSCs), and iPSC-derived
241 h as human mesenchymal stem cells (MSCs) and induced pluripotent stem cells (iPSCs), has not been ass
242 rst established a liver organoid using human induced pluripotent stem cells (iPSCs), mesenchymal stem
244 mechanisms of somatic reprogramming to human induced pluripotent stem cells (iPSCs), we have establis
245 pectedly, stem cells as well as reprogrammed induced pluripotent stem cells (iPSCs), where the protei
256 eprogramming by transcription factors (i.e., induced pluripotent stem cells, iPSCs) or by somatic cel
257 pproach using macrophages derived from human induced pluripotent stem cells (iPSdMs) to study macroph
258 ing cells from human embryonic stem cells or induced pluripotent stem cells is at present close to re
259 generated from multiple human embryonic and induced pluripotent stem cell lines and have potential a
260 S) in Parkinson's Disease, we have generated induced Pluripotent Stem Cell lines from early onset Par
261 s analyzing large-scale collections of human induced pluripotent stem cell lines provide valuable ins
267 ology, we established a ChAc patient-derived induced pluripotent stem cell model and an efficient dif
268 to nonsyndromic autism pathophysiology using induced pluripotent stem cells modeling disease technolo
270 ere, we reprogrammed fibroblasts to generate induced pluripotent stem cells, neural progenitor cells
272 ere we demonstrate the generation from human induced pluripotent stem cells of a self-formed ectoderm
275 ed from human neural progenitor cells, human induced pluripotent stem cells, or in primary rat cortic
277 ing skeletal muscle efficiently from porcine induced pluripotent stem cells (piPSC) in vitro thereby
278 from brain neurons, embryonic stem cells and induced pluripotent stem cells, primordial germ cells an
279 s and midbrain dopamine neurons derived from induced pluripotent stem cells, providing a novel model
280 ssue-engineering approach with embryonic and induced pluripotent stem cells (PSCs) to generate human
282 Targeted differentiation of patient-derived induced pluripotent stem cells showed a reduced expansio
284 and RA or retinol promote the derivation of induced pluripotent stem cells synergistically and enhan
285 etic Association Studies Consortium has used induced pluripotent stem cell technology to study the ef
286 ocytes that are derived from mouse and human induced pluripotent stem cells through a mechanism that
287 ning them with NPCs and neurons derived from induced pluripotent stem cells to create patient-specifi
288 ells that had been differentiated from human-induced pluripotent stem cells to generate a human-induc
290 ensional retinal tissue from patient-derived induced pluripotent stem cells to identify how CEP290 mu
291 cardiomyocytes generated from embryonic and induced pluripotent stem cells, to model newly formed ce
292 ns of early development in TSC, we generated induced pluripotent stem cells using dermal fibroblasts
296 reprogrammed from 3 persons with STGD1 into induced pluripotent stem cells, which were differentiate
297 e generated CSC-like cells by treating mouse induced pluripotent stem cells with conditioned medium f
298 show that human cardiomyocytes derived from induced pluripotent stem cells with enhanced expression
299 ions, both human cardiomyocytes derived from induced pluripotent stem cells with enhanced Kir2.1 expr
300 lls with an extra human chromosome and human induced pluripotent stem cells with trisomy 21, as well
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